Anemia is a common sign in both inpatient and outpatient settings and is defined as a decrease in the number of circulating red blood cells or hemoglobin. Oftentimes anemia is not evaluated or managed adequately. It is routinely listed as a freestanding diagnosis, however, it is in fact a clinical sign indicating the presence of an underlying etiology and additional workup is required to elucidate its cause. Anemia leads to diminished tissue oxygenation and can worsen the progression of many coexisting diseases. Despite this, there remains clinical discordance in both the formal definition of anemia and in protocols to screen for it [1][2][3].
Symptoms of anemia are diverse and can include fatigue, weakness, lightheadedness, headache, pallor or jaundice, tachycardia, palpitations, chest pain, dyspnea, cold distal extremities, and claudication. These signs and symptoms vary in prevalence and magnitude.
Anemia causes a decrease in the relative number of circulating red blood cells or hemoglobin, which leads to a consequent decrease in the amount of oxygen delivered to tissues. However, the hemoglobin concentration constituting anemia varies based on factors such as gender, ethnicity, and age. In addition, opinions differ as to which patient populations should undergo routine screening for anemia. Finally, the threshold for initiating treatment and the goals of treatment are subject to variation according to discipline and medical condition [4][5][6].
In 2010, the World Health Organization (WHO) criteria for diagnosing anemia required hemoglobin levels less than 12 grams per deciliter (g/dl) in premenopausal females and 13 g/dl in postmenopausal females and males of all ages. The journal Blood disagreed with these standards, citing the paucity of WHO data and proposed new thresholds for anemia based on race, gender and age. These proposed standards defined anemia as hemoglobin levels of less than 13.7 g/dl for white men between 20 and 60 years of age, less than 13.2 g/dl for white men older than 60, and white women of all ages were considered anemic at 12.2 g/dl. Although this journal did reference a significant difference in hemoglobin levels in black men and women, no standard levels for the diagnosis of anemia in these populations were proposed. Currently, the majority of the literature utilizes the WHO standards for consistency.
There is a similar discordance concerning screening for anemia between the US Preventative Services Task Force (USPTF), various individual medical academic institutions, and what is done in the day-to-day practice of medicine. For example, the USPTF issued a statement on screening for iron deficiency anemia in asymptomatic children between 6 and 24 months of age, stating that there was insufficient evidence on the benefits versus harms of screening for anemia in children in this age group. At the same time, the American Academy of Family Practice released its position statement: "Universal screening for anemia should be performed at 12 months of age, with measurement of hemoglobin levels and an assessment of risk factors associated with iron deficiency and iron-deficiency anemia."[7][1][8] The issue of screening in pregnant women presented a similar discordance. "The USPTF concludes that the evidence of the effect of routine screening for iron deficiency anemia in asymptomatic pregnant women on maternal health and birth outcomes is insufficient...and the balance of benefits and harms cannot be determined." The American Academy of Family Practice voiced agreement with the USPSTF. The American College of Obstetrics and Gynecology in Practice Bulletin No. 95 issued the position statement, "All pregnant women should be screened for anemia and treated if necessary." At present, there are no recommendations for routine anemia screening of non-gravid, well adults.
Anemia has multiple etiologies that can be attributed to one of 3 processes:
The above processes can be further subdivided into their specific causative etiologies. These include but are not limited to:
Epidemiological reporting of anemia is fragmented because of the use of different diagnostic criteria in the United States as opposed to the WHO criteria used for the rest of the world. Also, demographic subsets, genetic subsets and geographic subsets of anemia prevalence exist. Best estimates indicate that anemia prevalence is statistically similar in the United States, Canada, and northern Europe, and around 4% of males and 8% of females qualify for the diagnosis of anemia in these territories. There is substantially more limited data for the rest of the world. Estimates from the available data are inexact but do suggest that anemia frequency is between 2 and 5 times greater worldwide than in the US, Canada, and northern Europe.[9][10][11]
Regions in which populations commonly show higher rates of anemia include:
Red Blood Cells (RBC)
RBCs are released from the bone marrow as reticulocytes. The reticulocytes have a network of ribosomal RNA (rRNA) and over a period of 24 hours mature into adult RBCs. The relative reticulocyte count can be used to gauge whether the bone marrow is responding appropriately to anemia by increasing production. The RBC contains 2 alpha and 2 beta chains and a single heme moiety that reversibly binds oxygen. Although there are multiple possible genetic variants leading to an alteration in the configuration of these chains, most do not lead to clinical consequences. However, sickle cell disease and thalassemia variants of alpha and beta chains are causes of anemia. Genetic variants in the cell membrane, cell metabolism, and cell morphology are additional causes of anemia.
Bone Marrow
The bone marrow requires approximately 21 days transitioning a pluripotent stem cell to a reticulocyte released into circulation. The initial stimulus for reticulocyte production is the renal release of erythropoietin, and continued erythropoietin is required for the transformation of a pluripotent stem cell into a proerythroblast. This initial stage takes approximately 10 to 15 days. The next step is iron-dependent and takes 3-4 days, during which iron is added to the proerythroblast, forming a heme moiety and completing the formation of the reticulocyte.
Significant bone marrow related causes of anemia include:
Kidney
The kidneys have a dual role in the pathophysiology of anemia. Firstly, they are responsible for the production of 90% of the erythropoietin needed to stimulate bone marrow transformation of pluripotent stem cells to proerythroblasts. Interference with erythropoietin production and release will result in anemia. Secondly, acute anemia associated with acute blood loss results in hypotension, which causes the stimulation of stretch receptors, which in turn sends signals to parts of the brain via the glossopharyngeal and vagus nerve that lead to several downstream effects, including antidiuretic hormone (ADH), also known as arginine vasopressin (AVP) or vasopressin secretion. In response, the kidney reabsorbs water, in turn leading to decreased renal perfusion. In direct response to the decreased renal perfusion, the renin-angiotensin system becomes activated, leading to increased vascular tone and stimulation of aldosterone and resultant increased intravascular volume.
Central Nervous System (CNS)
The medulla, cerebral cortex, and pituitary gland coordinate the response to acute blood-loss anemia and the resultant volume changes by increasing sympathetic tone and secreting ADH.
The Acuity of Onset of the Anemia
Acute onset anemia due to blood loss or rapid hemolysis is compensated by the CNS-directed, renal-mediated response to the loss of volume and perfusion. This compensatory mechanism has an upper threshold and is well defined by The American College of Surgeons' Advanced Trauma Life Support (ATLS) protocols for management of volume loss:
On the other hand, very low hemoglobin may be tolerated in the setting of chronic, slowly progressing anemia wherein the RBC mass is greatly decreased but circulating blood volume is preserved. Management of blood products and anemia specific therapy, such as therapy with RBC substrates or erythropoietin, varies by case and by cause.
The array of laboratory testing and imaging that may be pertinent in the evaluation of anemia include:
Thorough patient history and physical exam are necessary to direct diagnostic testing and subsequent treatment. In the case of obvious cues on history or physical exam, the workup can be streamlined and focused and appropriate therapy implemented. If the etiology of anemia is not obvious, generalized diagnostic testing is used to narrow potential causes.
The differential for anemia is broad and includes:
The first question to ask is whether the patient is actively bleeding and, if so, how much. This will help determine the need for rapid should intervention. ATLS outlines clear guidelines to treat trauma-related hemorrhage. The most common non-traumatic causes of hemorrhage include gastrointestinal (GI), gynecologic (GYN), and genitourinary (GU) bleeding. The patient's hemodynamic stability is a primary guide to ensuring appropriate intervention. More subtle hemorrhage can be observed with anticoagulation and occult chest, abdominal, or pelvic bleeding or hematoma formation. As always, treatment is aimed at restoring blood volume and treating the cause of the bleeding.
If acute hemorrhage is deemed unlikely, it is important to categorize the anemia by cell size and hemoglobin density and to look at red blood cell morphology on peripheral smear. Anemia falls into the categories of macrocytic, microcytic and normocytic based on RBC size and hypo or normochromic based on relative hemoglobin concentration. Characteristic cell dysmorphisms may also be evident on a blood smear. An additional view of red cell dysmorphism can be elicited with hemoglobin electrophoresis to define the cell structure at the level of the amino acid chains binding the heme moiety.
Two additional fundamental questions are:
With the above data in hand, algorithms are applied based on red blood cell size:
Per the American Acadamy of Family Medicine (AAFP) position statement issued on March 15, 2011:
"Transfusion of RBCs should be based on the patient's clinical condition. Indications for RBC transfusion include acute sickle cell crisis, or acute blood loss of greater than 1500 cc or 30% of blood volume. Patients with symptomatic anemia should be transfused if they cannot function without treating the anemia."
The authors go on to site an updated Cochrane review supporting the use of a restrictive transfusion trigger in non-cardiac patients that supports maintaining hemoglobin levels of at least 7 g/dl. This more restrictive criterion is a significant change from the previously cited 10 g/dl threshold. Statistical analysis supports the 7 g/dl threshold, demonstrating a 54% relative decrease in the number of units of blood transfused and decreased 30-day mortality rate with implementation of the new criterion.
In conclusion, anemia is a sign that warrants further evaluation to determine its underlying etiology. It must be appreciated for both its primary medical impact on the patient and the potential secondary impact on the patient's comorbidities.
The diagnosis of anemia and its management is interprofessional. Anemia is a sign that needs to evaluated to determine its underlying etiology and must be appreciated for both its primary medical impact on the patient and its secondary impact on the patient's comorbidities. Thorough patient history and physical exam are necessary to direct diagnostic testing and subsequent treatment. In the case of obvious cues on history or physical exam, the workup can be streamlined and focused on clear therapeutic choices. Interprofessional healthcare team members that suspect a patient has anemia should further evaluate for it and in some cases, seek consultation from a hematologist.
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